LOINC Code 34493-7: PRF1 gene targeted mutation analysis Molgen Doc (Amn fld)

What is this code?

LOINC codes identify tests, measurements, observations, survey items, and clinical questions in a standardized way. It is associated with the component PRF1 gene targeted mutation analysis. It is commonly used with the system or sample type Amnio fld.

When is it used?

• Used in lab systems, EHRs, and clinical data exchange.
• May identify a test, observation, survey item, or clinical document request rather than a diagnosis.
• Status: ACTIVE
• Order vs observation: Both
• Method: Molgen

What it does not mean

• The code identifies the observation or test, not the actual result.

Key facts

• PRF1 gene targeted mutation analysis in Amniotic fluid by Molecular genetics method
• PRF1 gene targeted mutation analysis
• AF; Amn; Amn fl; Amnio; Amniotic flu; Amniotic fluid; Document; Finding; Findings; FLH2; Genetics; Gyn; Gynecology; Heredity; Heritable; HPLH2; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; OB; ObGyn; Obstetrics; P1; PCR; Perforin 1; perforin 1 (pore forming protein); PFN1; PFP; Point in time; Pore forming protein gene; preforming protein; Random

Where you may see this code

You may see this code in lab systems, lab reports, EHR exports, interoperability feeds, or other structured clinical data exchanges.

Common synonyms

Frequently asked questions